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Charcot–Marie–Tooth disease (CMT) is the most common inherited neuromuscular disorder, characterized by genetic heterogeneity and variable disease progression. Diagnosis involves clinical assessment, nerve-conduction studies, and DNA testing, with no current drug therapies available, although rehabilitation and surgical options exist. Ongoing research aims to identify effective treatments, with promising results from experimental models using various compounds, including ascorbic acid, currently under inves

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emillyrfm

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